Canonical Allele Identifier: CA16615785
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409314
dbSNP Id: rs1064792958

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094724_43094735delinsT , CM000679.2:g.43094724_43094735delinsT GRCh38
NC_000017.10:g.41246741_41246752delinsT , CM000679.1:g.41246741_41246752delinsT GRCh37
NC_000017.9:g.38500267_38500278delinsT NCBI36
NG_005905.2:g.123249_123260delinsA , LRG_292:g.123249_123260delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.860_871delinsA
ENST00000461574.2:c.796_807delinsA ENSP00000417241.2:p.Val266ThrfsTer17
ENST00000470026.6:c.796_807delinsA ENSP00000419274.2:p.Val266ThrfsTer17
ENST00000473961.6:c.670_681delinsA ENSP00000420201.2:p.Val224ThrfsTer17
ENST00000476777.6:c.793_804delinsA ENSP00000417554.2:p.Val265ThrfsTer17
ENST00000477152.6:c.718_729delinsA ENSP00000419988.2:p.Val240ThrfsTer17
ENST00000478531.6:c.784+9_784+20delinsA ENSP00000420412.2:n.784+9_784+20delinsA
ENST00000489037.2:c.718_729delinsA ENSP00000420781.2:p.Val240ThrfsTer17
ENST00000493919.6:c.646+9_646+20delinsA ENSP00000418819.2:n.646+9_646+20delinsA
ENST00000494123.6:c.796_807delinsA ENSP00000419103.2:p.Val266ThrfsTer17
ENST00000497488.2:c.-93_-82delinsA ENSP00000418986.2:n.-93_-82delinsA
ENST00000618469.2:c.796_807delinsA ENSP00000478114.2:p.Val266ThrfsTer17
ENST00000634433.2:c.673_684delinsA ENSP00000489431.2:p.Val225ThrfsTer17
ENST00000644379.2:c.796_807delinsA ENSP00000496570.2:p.Val266ThrfsTer17
ENST00000644555.2:c.646+9_646+20delinsA ENSP00000494614.2:n.646+9_646+20delinsA
ENST00000652672.2:c.655_666delinsA ENSP00000498906.2:p.Val219ThrfsTer17
ENST00000484087.6:c.664+9_664+20delinsA ENSP00000419481.2:n.664+9_664+20delinsA
ENST00000700182.1:c.706+9_706+20delinsA ENSP00000514849.1:n.706+9_706+20delinsA
ENST00000700183.1:c.*804_*815delinsA ENSP00000514850.1:n.*804_*815delinsA
ENST00000357654.9:c.796_807delinsA MANE Select ENSP00000350283.3:p.Val266ThrfsTer17
ENST00000471181.7:c.796_807delinsA ENSP00000418960.2:p.Val266ThrfsTer17
ENST00000642945.1:c.*670_*681delinsA ENSP00000495897.1:n.*670_*681delinsA
ENST00000652672.1:c.655_666delinsA ENSP00000498906.1:p.Val219ThrfsTer17
ENST00000352993.7:c.670+1111_670+1122delinsA ENSP00000312236.5:n.670+1111_670+1122deli...
ENST00000354071.7:c.796_807delinsA ENSP00000326002.7:p.Val266ThrfsTer17
ENST00000357654.7:c.796_807delinsA ENSP00000350283.3:p.Val266ThrfsTer17
ENST00000412061.3:c.147_158delinsA
ENST00000461221.5:c.*579_*590delinsA ENSP00000418548.1:n.*579_*590delinsA
ENST00000468300.5:c.787+9_787+20delinsA ENSP00000417148.1:n.787+9_787+20delinsA
ENST00000470026.5:c.796_807delinsA ENSP00000419274.1:p.Val266ThrfsTer17
ENST00000471181.6:c.796_807delinsA ENSP00000418960.2:p.Val266ThrfsTer17
ENST00000473961.5:c.393_404delinsA
ENST00000477152.5:c.718_729delinsA ENSP00000419988.1:p.Val240ThrfsTer17
ENST00000478531.5:c.784+9_784+20delinsA ENSP00000420412.1:n.784+9_784+20delinsA
ENST00000484087.5:c.409+9_409+20delinsA ENSP00000419481.1:n.409+9_409+20delinsA
ENST00000487825.5:c.412+9_412+20delinsA ENSP00000418212.1:n.412+9_412+20delinsA
ENST00000491747.6:c.787+9_787+20delinsA ENSP00000420705.2:n.787+9_787+20delinsA
ENST00000492859.5:c.*732_*743delinsA ENSP00000420253.1:n.*732_*743delinsA
ENST00000493795.5:c.655_666delinsA ENSP00000418775.1:p.Val219ThrfsTer17
ENST00000493919.5:c.646+9_646+20delinsA ENSP00000418819.1:n.646+9_646+20delinsA
ENST00000494123.5:c.796_807delinsA ENSP00000419103.1:p.Val266ThrfsTer17
ENST00000497488.1:c.-93_-82delinsA ENSP00000418986.1:n.-93_-82delinsA
ENST00000586385.5:c.4+30447_4+30458delinsA ENSP00000465818.1:n.4+30447_4+30458delins...
ENST00000591534.5:c.-43-20214_-43-20203delinsA ENSP00000467329.1:n.-43-20214_-43-20203de...
ENST00000591849.5:c.-99+30536_-99+30547delinsA ENSP00000465347.1:n.-99+30536_-99+30547de...
ENST00000634433.1:c.673_684delinsA ENSP00000489431.1:p.Val225ThrfsTer17
NM_007294.3:c.796_807delinsA , LRG_292t1:c.796_807delinsA NP_009225.1:p.Val266ThrfsTer17
NM_007297.3:c.655_666delinsA NP_009228.2:p.Val219ThrfsTer17
NM_007298.3:c.787+9_787+20delinsA NP_009229.2:n.787+9_787+20delinsA
NM_007299.3:c.787+9_787+20delinsA NP_009230.2:n.787+9_787+20delinsA
NM_007300.3:c.796_807delinsA NP_009231.2:p.Val266ThrfsTer17
NR_027676.1:n.932_943delinsA
NM_007294.4:c.796_807delinsA MANE Select NP_009225.1:p.Val266ThrfsTer17
NM_007297.4:c.655_666delinsA NP_009228.2:p.Val219ThrfsTer17
NM_007299.4:c.787+9_787+20delinsA NP_009230.2:n.787+9_787+20delinsA
NM_007300.4:c.796_807delinsA NP_009231.2:p.Val266ThrfsTer17
NR_027676.2:n.973_984delinsA